The Medical Letter on Drugs and Therapeutics
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1503
Daclizumab (Zinbryta) for Multiple Sclerosis
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Revised 3/6/18: Withdrawn from the market March 2018 due to safety concerns.

The FDA has approved daclizumab (Zinbryta – Biogen/Abbvie), an interleukin-2 (IL-2) receptor blocking monoclonal antibody, for treatment of adults with relapsing forms of multiple sclerosis (MS). It is the first subcutaneously injected monoclonal antibody to be approved for treatment of MS.

Because of safety concerns, the label recommends that daclizumab generally be used only for patients who have had an inadequate response to ≥2 other MS drugs, and its availability is restricted by a Risk Evaluation and Mitigation Strategy (REMS) program. Zenapax, an earlier IV formulation of daclizumab, was approved by the FDA in 1997 for prevention of acute renal transplant rejection,1 but it is no longer marketed.

TREATMENT OF MS — Interferons have been used for first-line treatment of MS, but they appear to be less effective than some of the newer drugs and ... more      

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Title: Daclizumab (Zinbryta) for Multiple Sclerosis
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